8-[(Triphenylphosphonio)methyl]-5,6-bis(hydroxymethyl)-2,2-dimethyl-4H-[1,3]dioxino[4,5-c]pyridin chloride

ID: ALA2398194

PubChem CID: 71723465

Max Phase: Preclinical

Molecular Formula: C30H31ClNO4P

Molecular Weight: 500.56

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC1(C)OCc2c(CO)c(CO)nc(C[P+](c3ccccc3)(c3ccccc3)c3ccccc3)c2O1.[Cl-]

Standard InChI:  InChI=1S/C30H31NO4P.ClH/c1-30(2)34-20-26-25(18-32)27(19-33)31-28(29(26)35-30)21-36(22-12-6-3-7-13-22,23-14-8-4-9-15-23)24-16-10-5-11-17-24;/h3-17,32-33H,18-21H2,1-2H3;1H/q+1;/p-1

Standard InChI Key:  WKCGRTPZDQVGOH-UHFFFAOYSA-M

Molfile:  

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  2  3  1  0
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M  CHG  2   1  -1  19   1
M  END

Associated Targets(non-human)

Proteus (150 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 500.56Molecular Weight (Monoisotopic): 500.1985AlogP: 4.21#Rotatable Bonds: 7
Polar Surface Area: 71.81Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.90CX Basic pKa: 2.27CX LogP: 3.69CX LogD: 3.69
Aromatic Rings: 4Heavy Atoms: 36QED Weighted: 0.37Np Likeness Score: 0.44

References

1. Pugachev MV, Shtyrlin NV, Sysoeva LP, Nikitina EV, Abdullin TI, Iksanova AG, Ilaeva AA, Musin RZ, Berdnikov EA, Shtyrlin YG..  (2013)  Synthesis and antibacterial activity of novel phosphonium salts on the basis of pyridoxine.,  21  (14): [PMID:23683836] [10.1016/j.bmc.2013.04.051]

Source